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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46555Erstellt: 23. Oktober 2026

Bromine → 2-Bromo-1-(3,4-difluorophenyl)ethan-1-one

https://huagongshe.com/de/reaction/46555

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromineHCID 24408—
Edukt2-Bromo-1-(2,4-dichlorophenyl)ethan-1-oneHCID 75828—
Edukt1-(3,4-Difluorophenyl)ethan-1-oneHCID 123052—
Edukt2-Bromo-1-(2,5-difluorophenyl)ethanoneHCID 2778264—
Edukt2-Bromo-1-(3,4-diethoxyphenyl)ethan-1-oneHCID 3492104—
Edukt2-Bromo-1-(3,4-dimethylphenyl)ethan-1-oneHCID 3703113—
Edukt2-Bromo-1-(4-(propan-2-yl)phenyl)ethan-1-oneHCID 14042756—
Edukt2-Bromo-1-(4-(propan-2-yloxy)phenyl)ethan-1-oneHCID 15453912—
Eduktm-Isobutylphenacyl bromideHCID 20387511—
Edukt2-Bromo-1-(3-ethoxyphenyl)ethanoneHCID 22641006—
Edukt2-Bromo-1-(2-ethylphenyl)ethan-1-oneHCID 23442601—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelChloroformHCID 6212—
Produkt2-Bromo-1-(3,4-difluorophenyl)ethan-1-oneHCID 2737032—

Reaktionsschritte

To a solution of 10.1 g. (0.065 mole) of 3,4-difluoroacetophenone in 100 ml. of glacial acetic acid was added 3.4 ml. (0.065 mole) of bromine dropwise. When the addition was complete the solution was stirred for 0.5 hr. and then stripped to dryness under reduced pressure. The residue was dissolved in chloroform and washed with aqueous sodium bicarbonate. Evaporation of the organic phase provided 14.8 g. (97%) of colorless liquid product. Similarly prepared were 2,4-dichlorophenacyl bromide, o-ethylphenacyl bromide, p-isopropylphenacyl bromide, m-isobutylphenacyl bromide, 3,4-dimethylphenacyl bromide, m-ethoxyphenacyl bromide, p-isopropoxyphenacyl bromide, 3,4-diethoxyphenacyl bromide, and 2,5-difluorophenacyl bromide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04173650
Quelldatensatzuspto-grants-1979_11
ORD IDord-51ac15fa7aa84ece864078149c112857
Quellennotizuspto-grants-1979_11